We are looking for a CQV Engineer to join our Quality Compliance team.

Mobility : France

Group 10
Responsibilities

  • Perform Commissioning, Qualification, Validation team activities with a direct regard for Safety.
  • Generate C&Q Procedures for projects.
  • Review/qualify lab equipment.
  • Writes, review and revise a variety of Installation, Operation and Performance qualification/verification related documents, including any of all of the following: SOPs, validation/verification master plans, guidelines and execution plans
  • Facilitate scoping / planning of commissioning spares and consumables.
  • Deliver the C&Q activities as required to meet the schedule
  • Track progress of C&Q activities as required.
  • Execution of Design reviews, shakedown, commissioning, FAT’s, IQ, OQ, PQ activities.
  • Coordinate with project contractors and equipment vendors to execute required tests.
  • Allocate project resources for efficient execution of project deliverables.
  • Coordinate support during C&Q execution

Group 12
Profile

  • BS or MS in a relevant science or engineering field, or equivalent
  • From 3 years of experience in CQV excluding internship and apprenticeship
  • Excellent oral and written communication skills
  • Excellent problem-solving skills
  • Customer-service focused.
  • Proficient in life science manufacturing processes in areas such as biotech, aseptic fill/finish, OSD, Gene Therapy or equivalent experience.

CQV Engineer

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